Canonical Allele Identifier: CA385782136
Gene: TPH2 HGNC NCBI

Linked Data

gnomAD v4: 12-71994530-G-A
MyVariant Identifiers: chr12:g.72388310G>A (hg19) chr12:g.71994530G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71994530G>A , CM000674.2:g.71994530G>A GRCh38
NC_000012.11:g.72388310G>A , CM000674.1:g.72388310G>A GRCh37
NC_000012.10:g.70674577G>A NCBI36
NG_008279.1:g.60685G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000333850.4:c.1033G>A MANE Select ENSP00000329093.3:p.Gly345Arg
ENST00000333850.3:c.1033G>A ENSP00000329093.3:p.Gly345Arg
NM_173353.3:c.1033G>A NP_775489.2:p.Gly345Arg
XM_011537899.1:c.439G>A XP_011536201.1:p.Gly147Arg
NM_173353.4:c.1033G>A MANE Select NP_775489.2:p.Gly345Arg
Search 100 bp 5'
Search 100 bp 3'